FDA Inspection 1063752 — Global Flex Bed, Inc.

Global Flex Bed, Inc. — FEI 3009965344

The FDA completed an inspection of Global Flex Bed, Inc. on Jun 21, 2018 in La Mirada, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
La Mirada, CA (United States)